日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Predictive value of vascular endothelial growth factor polymorphisms for maintenance bevacizumab efficacy in metastatic colorectal cancer: an ancillary study of the PRODIGE 9 phase III trial

血管内皮生长因子多态性对转移性结直肠癌贝伐单抗维持疗效的预测价值:PRODIGE 9 III期试验的辅助研究

de Rauglaudre, Bernadette; Sibertin-Blanc, Camille; Fabre, Aurélie; Le Malicot, Karine; Bennouna, Jaafar; Ghiringhelli, François; Taïeb, Julien; Boige, Valérie; Bouché, Olivier; Chatellier, Thierry; Faroux, Roger; François, Eric; Jacquot, Stéphane; Genet, Dominique; Mulot, Claire; Olschwang, Sylviane; Seitz, Jean-François; Aparicio, Thomas; Dahan, Laetitia

Pan Aurora Kinase Inhibitor: A Promising Targeted-Therapy in Dedifferentiated Liposarcomas With Differential Efficiency Depending on Sarcoma Molecular Profile

泛极光激酶抑制剂:一种有前景的去分化脂肪肉瘤靶向疗法,其疗效差异取决于肉瘤分子特征

Jean Camille Mattei, Corinne Bouvier-Labit, Doriane Barets, Nicolas Macagno, Mathieu Chocry, Frédéric Chibon, Philippe Morando, Richard Alexandre Rochwerger, Florence Duffaud, Sylviane Olschwang, Sébastien Salas, Carine Jiguet-Jiglaire

Genomic profile concordance between pancreatic cyst fluid and neoplastic tissue

胰腺囊液与肿瘤组织的基因组谱一致性

Laquière, Arthur E; Lagarde, Arnaud; Napoléon, Bertrand; Bourdariat, Raphaël; Atkinson, Alexandre; Donatelli, Gianfranco; Pol, Bernard; Lecomte, Laurence; Curel, Laurence; Urena-Campos, Romina; Helbert, Thierry; Valantin, Vincent; Mithieux, François; Buono, Jean Pascal; Grandval, Philippe; Olschwang, Sylviane

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations

癌症基因基因组测序次要发现报告指南:SFMPP建议

Pujol, Pascal; Vande Perre, Pierre; Faivre, Laurence; Sanlaville, Damien; Corsini, Carole; Baertschi, Bernard; Anahory, Michèle; Vaur, Dominique; Olschwang, Sylviane; Soufir, Nadem; Bastide, Noëlle; Amar, Sarah; Vintraud, Michèle; Ingster, Olivier; Richard, Stéphane; Le Coz, Pierre; Spano, Jean-Philippe; Caron, Olivier; Hammel, Pascal; Luporsi, Elisabeth; Toledano, Alain; Rebillard, Xavier; Cambon-Thomsen, Anne; Putois, Olivier; Rey, Jean-Marc; Hervé, Christian; Zorn, Caroline; Baudry, Karen; Galibert, Virginie; Gligorov, Joseph; Azria, David; Bressac-de Paillerets, Brigitte; Burnichon, Nelly; Spielmann, Marc; Zarca, Daniel; Coupier, Isabelle; Cussenot, Olivier; Gimenez-Roqueplo, Anne-Paule; Giraud, Sophie; Lapointe, Anne-Sophie; Niccoli, Patricia; Raingeard, Isabelle; Le Bidan, Muriel; Frebourg, Thierry; Rafii, Arash; Geneviève, David

Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndrome

突尼斯一名患者罕见病合并症的临床特征:色素失禁症和努南综合征病例报告

Ghedira, Nehla; Lagarde, Arnaud; Ben Ameur, Karim; Elouej, Sahar; Sakka, Rania; Kerkeni, Emna; Chioukh, Fatma-Zohra; Olschwang, Sylviane; Desvignes, Jean-Pierre; Abdelhak, Sonia; Delague, Valerie; Lévy, Nicolas; Monastiri, Kamel; De Sandre-Giovannoli, Annachiara

Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

APC基因1B外显子中的点突变揭示胃腺癌和胃近端息肉病是家族性腺瘤性息肉病的一种变异型

Li, Jun; Woods, Susan L; Healey, Sue; Beesley, Jonathan; Chen, Xiaoqing; Lee, Jason S; Sivakumaran, Haran; Wayte, Nicci; Nones, Katia; Waterfall, Joshua J; Pearson, John; Patch, Anne-Marie; Senz, Janine; Ferreira, Manuel A; Kaurah, Pardeep; Mackenzie, Robertson; Heravi-Moussavi, Alireza; Hansford, Samantha; Lannagan, Tamsin R M; Spurdle, Amanda B; Simpson, Peter T; da Silva, Leonard; Lakhani, Sunil R; Clouston, Andrew D; Bettington, Mark; Grimpen, Florian; Busuttil, Rita A; Di Costanzo, Natasha; Boussioutas, Alex; Jeanjean, Marie; Chong, George; Fabre, Aurélie; Olschwang, Sylviane; Faulkner, Geoffrey J; Bellos, Evangelos; Coin, Lachlan; Rioux, Kevin; Bathe, Oliver F; Wen, Xiaogang; Martin, Hilary C; Neklason, Deborah W; Davis, Sean R; Walker, Robert L; Calzone, Kathleen A; Avital, Itzhak; Heller, Theo; Koh, Christopher; Pineda, Marbin; Rudloff, Udo; Quezado, Martha; Pichurin, Pavel N; Hulick, Peter J; Weissman, Scott M; Newlin, Anna; Rubinstein, Wendy S; Sampson, Jone E; Hamman, Kelly; Goldgar, David; Poplawski, Nicola; Phillips, Kerry; Schofield, Lyn; Armstrong, Jacqueline; Kiraly-Borri, Cathy; Suthers, Graeme K; Huntsman, David G; Foulkes, William D; Carneiro, Fatima; Lindor, Noralane M; Edwards, Stacey L; French, Juliet D; Waddell, Nicola; Meltzer, Paul S; Worthley, Daniel L; Schrader, Kasmintan A; Chenevix-Trench, Georgia

Clinical Utility Gene Card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP)--update 2014

家族性腺瘤性息肉病 (FAP) 和衰减型家族性腺瘤性息肉病 (AFAP) 的临床实用基因卡——2014 年更新

Aretz, Stefan; Vasen, Hans F A; Olschwang, Sylviane

Molecular patterns in deficient mismatch repair colorectal tumours: results from a French prospective multicentric biological and genetic study

错配修复缺陷结肠直肠肿瘤的分子模式:法国前瞻性多中心生物和遗传学研究的结果

M-C Etienne-Grimaldi, A Mahamat, M Chazal, P Laurent-Puig, S Olschwang, M-P Gaub, J-L Formento, P Formento, A Sudaka, V Boige, A Abderrahim-Ferkoune, D Benchimol, T André, S Houry, J-L Faucheron, C Letoublon, F-N Gilly, J-R Delpero, P Lasser, B Pradere, D Pezet, F Penault-Llorca, G Milano

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012

林奇综合征(MLH1、MSH2、MSH6、PMS2、EPCAM)临床实用基因卡 - 2012 年更新

Rahner, Nils; Steinke, Verena; Schlegelberger, Brigitte; Eisinger, Francois; Hutter, Pierre; Olschwang, Sylviane

UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families

UMD-MLH1/MSH2/MSH6 数据库:法国林奇综合征家族遗传变异的描述和分析

Grandval, Philippe; Fabre, Aurélie J; Gaildrat, Pascaline; Baert-Desurmont, Stéphanie; Buisine, Marie-Pierre; Ferrari, Anthony; Wang, Qing; Béroud, Christophe; Olschwang, Sylviane